The following packages were found for maintainer: bacon@NetBSD.org
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wip/bolt-lmm Statistics for testing association between phenotype and genotypes
wip/fastahack Utilities for indexing and sequence extraction from FASTA files
wip/fastqc Quality control tool for high throughput sequence data
wip/py-eggnog-mapper Fast functional annotation of novel DNA or protein sequences
wip/py-dnaio Read and write FASTQ and FASTA files
wip/gemma Genome-wide Efficient Mixed Model Association
wip/fastaunique Sort and uniq fasta files
wip/readseq Read and reformat biosequences, Java command-line version
wip/pkg-dev Scripts to automate common tasks in pkgsrc development
wip/bpcscripts Gast Illumina processing
biology/biolibc Low-level high-performance bioinformatics library
biology/plink Whole-genome association analysis toolset
biology/gffread GFF/GTF format conversions, filtering, FASTA extraction, etc
wip/epacts Efficient and Parallelizable Association Container Toolbox
biology/bedtools Swiss army knife for genome arithmetic
biology/vcf-split Split a multi-sample VCF into single-sample VCFs
archivers/libaec Adaptive entropy coding library
biology/biolibc-tools High-performance bioinformatics tools based on biolibc
wip/centrifuge Novel microbial classification engine
wip/canu Single molecule sequence assembler for genomes large and small
biology/fastp Ultra-fast all-in-one FASTQ preprocessor
biology/canu Single molecule sequence assembler for genomes large and small
security/munge Authentication service for creating and validating credentials
biology/samtools Tools for manipulating sequence alignment maps
biology/atac-seq Core tools needed for ATAC-Seq analysis
www/webbrowser Proxy script for launching best available web browser
wip/structure Multi-locus genotype data to investigate population structure
devel/simde Header-only library for SIMD intrinsics
wip/libgtextutils Gordon text utilities
devel/libgtextutils Gordon text utilities
math/basic-stats Command-line tool to perform basic statistics on tabular data
biology/kallisto Quantify abundances of transcripts from RNA-Seq data
biology/htslib C library for high-throughput sequencing data formats
wip/vcf2hap Generate .hap file from VCF for haplohseq
wip/plasm Portable Assembler
wip/fasda Fast and simple differential analysis
biology/generand Generate random genomic data in FASTA/FASTQ, SAM, or VCF format
biology/hisat2 Alignment program for mapping next-generation sequencing reads
biology/fastx-toolkit CLI tools for Short-Reads FASTA/FASTQ files preprocessing
biology/cdhit Clustering and comparing protein or nucleotide sequences
biology/vsearch Versatile open-source tool for metagenomics
devel/libxtend Miscellaneous functions to extend libc
wip/stacks Software pipeline for building loci from short-read sequences
wip/rsem RNA-Seq by Expectation-Maximization
wip/famsa Algorithm for large-scale multiple sequence alignments
wip/brain-mesh-builder Surface mesh building based on 3-dimensional image stacks
wip/py-macs2 Algorithm for identifying transcription factor binding sites
wip/samtools Tools for manipulating sequence alignment maps
wip/vcf-split Split a multi-sample VCF into single-sample VCFs
wip/cut-and-run Split a text file into segments and process in parallel
wip/ncbi-blast+ NCBI implementation of Basic Local Alignment Search Tool
wip/metal Meta-analysis of genomewide association scans
wip/py-dna-features-viewer Python library to visualize DNA features, e.g. GenBank or Gff files
wip/py-bcbio-gff Read and write Generic Feature Format (GFF) with Biopython integration
wip/auto-admin Portable tools for automating systems management
wip/libpare Pointer Array Regular Expressions
wip/fastq-trim Lightening fast sequence read trimmer
wip/microsynteny-tools Tools for exploring microsyntenic differences among species
wip/fastp Ultra-fast all-in-one FASTQ preprocessor
wip/slclust Single-linkage clustering with Jaccard similarity
wip/tabixpp C++ wrapper to tabix indexer
wip/atac-seq Core tools needed for ATAC-Seq analysis
wip/hisat2 Alignment program for mapping next-generation sequencing reads
wip/spcm Simple, portable cluster management
wip/wip-tools Tools for developing wip packages
wip/p5-transdecoder Identify candidate coding regions within transcript sequences
wip/fbsd2pkg Convert a FreeBSD port framework to a pkgsrc package
wip/py-pysam Python module for reading, manipulating and writing genomic data sets
wip/bio-mocha Bcftools plugin for mosaic chromosomal alteration analysis
wip/mst-bench Maximum sustainable throughput benchmark
wip/vsearch Versatile open-source tool for metagenomics
wip/lpjs Lightweight, Portable Job Scheduler
wip/bcftools Tools for manipulating BCF and VCF variant call files
wip/twintk Terminal Windows Toolkit
wip/fastx-toolkit CLI tools for Short-Reads FASTA/FASTQ files preprocessing
wip/seqtk Tool for processing sequences in FASTA/FASTQ format
wip/rna-seq Core tools needed for RNA-Seq analysis
wip/peak-classifier Classify ChIP/ATAC-Seq peaks based on features provided in a GFF
wip/gffread GFF/GTF format conversions, filtering, FASTA extraction, etc
wip/basic-stats Command-line tool to perform basic statistics on tabular data
wip/htslib C library for high-throughput sequencing data formats
wip/auto-dev Tools for automating code development and documentation
wip/libxtend Miscellaneous functions to extend libc
wip/papp Assembly Preprocessor
wip/bowtie2 Ultrafast, memory-efficient short read aligner
wip/biolibc Low-level high-performance bioinformatics library
wip/docviewer Generic command to automatically select a document viewer
wip/generand Generate random genomic data in FASTA/FASTQ, SAM, or VCF format
wip/biolibc-tools High-performance bioinformatics tools based on biolibc
biology/fastqc Quality control tool for high throughput sequence data
biology/fasda Fast and simple differential analysis
biology/ad2vcf Add allelic depth info from a SAM stream to a VCF file
biology/bwa Map low-divergent sequences against a large reference genome
biology/igv Visualization tool for genomic datasets
biology/py-macs2 Algorithm for identifying transcription factor binding sites
biology/vcf2hap Generate .hap file from VCF for haplohseq
biology/peak-classifier Classify ChIP/ATAC-Seq peaks based on features provided in a GFF
wip/ape Another Programmers Editor
biology/ncbi-blast+ NCBI implementation of Basic Local Alignment Search Tool
biology/stacks Software pipeline for building loci from short-read sequences
biology/plinkseq C/C++ library for working with human genetic variation data
biology/bowtie2 Ultrafast, memory-efficient short read aligner
biology/fastq-trim Lightening fast sequence read trimmer
wip/kallisto Quantify abundances of transcripts from RNA-Seq data
wip/bwa Map low-divergent sequences against a large reference genome
biology/seqtk Tool for processing sequences in FASTA/FASTQ format
sysutils/auto-admin Portable tools for automating systems management
wip/npmount Command line tool for non-privileged [un]mount
wip/qmediamanager GUI tool for managing removable media
wip/desktop-installer Quickly configure a NetBSD desktop system
sysutils/devpub-mount NetBSD devpubd-based automounter
sysutils/desktop-installer Quickly configure a NetBSD desktop system
wip/devpub-mount NetBSD devpubd-based automounter
biology/chip-seq Core tools needed for ChIP-Seq analysis
sysutils/npmount Command line tool for non-privileged [un]mount
sysutils/qmediamanager GUI tool for managing removable media
wip/py-multiqc Aggregate bioinformatics analysis reports across samples and tools
wip/stringtie Transcript assembly and quantification for RNA-seq
devel/py-rich-click Format click help output nicely with rich
graphics/py-spectra Color scales and color conversion made easy for Python
archivers/py-lzstring LZ-based in-memory string compression
biology/py-multiqc Aggregate bioinformatics analysis reports across samples and tools
devel/py-capturer Easily capture stdout/stderr of the current process and subprocesses
devel/py-verboselogs Extend Python logging module to add the log levels
devel/py-coloredlogs Colored terminal output for Pythons logging module
math/py-colormath Module that spares the user from directly dealing with color math
biology/rna-star Spliced Transcripts Alignment to a Reference
textproc/py-humanfriendly Human friendly output for text interfaces using Python
biology/stringtie Transcript assembly and quantification for RNA-seq
wip/sra-tools NCBIs toolkit for handling data in INSDC Sequence Read Archives
biology/bcftools Tools for manipulating BCF and VCF variant call files
biology/rna-seq Core tools needed for RNA-Seq analysis
biology/sra-tools NCBIs toolkit for handling data in INSDC Sequence Read Archives
sysutils/runas Wrapper around su for running a command as another user
wip/gcta Genome-wide Complex Trait Analysis
biology/py-bcbio-gff Read and write Generic Feature Format (GFF) with Biopython integration
biology/microsynteny-tools Tools for exploring microsyntenic differences among species
biology/py-dna-features-viewer Python library to visualize DNA features, e.g. GenBank or Gff files
wip/py-cython-legacy C-Extensions for Python
wip/chip-seq Core tools needed for ChIP-Seq analysis
math/armadillo C++ linear algebra library
devel/py-cykhash Cython equivalent to khash-sets/maps
biology/py-macs3 Peak caller aimed at transcription factor binding sites
wip/biostar-tools Meta-package for Biostar Handbook tools
biology/trimmomatic Flexible read trimming tool for Illumina NGS data
wip/pear Memory-efficient and highly accurate pair-end read merger
wip/fastool Simple and quick FastQ and FastA tool for file reading and conversion
wip/detab Replace tabs with spaces in a text file
wip/trimadap Trim adapter sequences from Illumina data using heuristic rules
biology/bio-mocha Bcftools plugin for mosaic chromosomal alteration analysis
biology/bcf-score Bcftools plugin for mosaic chromosomal alteration analysis
biology/mca-calling Core tools for Mosaic Chromosomal Alteration event calling
biology/haplohseq Identify regions of allelic imbalance
wip/rainbow Short reads clustering and local assembly
wip/gmap Genomic Mapping and Alignment Program for mRNA and EST Sequences
wip/igv Visualization tool for genomic datasets
wip/py-pybigwig Python access to bigWig files using libBigWig
wip/subread High-performance read alignment, quantification and mutation discovery
wip/fasttree Approximately-maximum-likelihood phylogenetic trees from alignments
wip/rna-star Spliced Transcripts Alignment to a Reference
wip/runas Wrapper around su for running a command as another user
wip/ad2vcf Add allelic depth info from a SAM stream to a VCF file
wip/filevercmp Filevercmp function as in sort --version-sort
wip/munge Authentication service for creating and validating credentials
wip/webbrowser Proxy script for launching best available web browser
wip/py-htseq Python library to facilitate programmatic analysis of sequence data
wip/ti99sim SDL-based TI-99/4a simulator
wip/bifrost Parallel construction, indexing and querying of de Bruijn graphs
wip/bcf-score Bcftools plugin for mosaic chromosomal alteration analysis
wip/py-macs3 Peak caller aimed at transcription factor binding sites
wip/muscle MUltiple Sequence Comparison by Log-Expectation
wip/bedtools Swiss army knife for genome arithmetic